FDA 510(k) Applications Submitted by COVIDIEN LP, FORMERLY KNOW AS VALLEYLAB, A DIVISON
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K110268 | 01/28/2011 | FORCETRIAD ELECTROSURGICAL GENERATOR | COVIDIEN LP, FORMERLY KNOW AS VALLEYLAB, A DIVISON |
| K072687 | 09/24/2007 | VALLEYLAB MICROWAVE ABLATION GENERATOR | COVIDIEN LP, FORMERLY KNOW AS VALLEYLAB, A DIVISON |
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